Allele Registry

Canonical Allele Identifier: PA2825769056

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000726094

RCV001139795

RCV001833380

RCV003155152

ClinVar Variation:

287943

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Arg388Trp	CA1705660 NM_001130986.2:c.1162C>T